Three methoxy-ether and one methoxy-ether/crown-ether derivatives of p-tert
-butyltetrahomodioxa- and p-R-octahomotetraoxacalix[4]arenes (R = methyl, t
ert-butyl, H) have been investigated. The first three compounds, 7,15,21,27
-tetra-tertbutyl-29,30,31,32-tetramethoxy-3,11-dioxapentacyclo[23.3.1.- 1(5
,9).1(13,17)1(19,23)]ditriaconta-1(29),5,7,9(30),13,15,-17(31),19,21,23(32)
,25,27-dodecaene, C50H68O6, 33,34,35,36-tetramethoxy-7,15,23,31-tetramethyl
-3,11,19,27-tetraoxapentacyclo[27.3.1.- 1(5,9).1(13,17).1(21,25)]hexatriaco
nta-1(33),5,7,9(34),13,15,17(35),21,23,25(36),29,31-dodecaene, C40H48O8, an
d 7,23-di-tert-butyl-33,34,35,36-tetramethoxy-3,11,19,27-tetraoxapentacyclo
[27.3.-1.1 (5,9).1(13,17).1(21,25)]hexatriaconta-1(33),5,7,9(34),13,15,17(3
5),21,23,25(36),29,31-dodecaene, C44H56O8, in the partial-cone or 1,2-alter
nate conformations, present the common feature of methoxy-ether self-inclus
ion, while the fourth, 42,43-dimethoxy-7,15,23,31-tetramethyl-3,11,19,27,34
,37,40-heptaoxa- hexacyclo[15.15.9.1(5,9).1(21,25).0(13,41).0(29,33)]tritet
raconta-5(42),6,8,13(41),14,16,21(43),22,24,29(33),30,32-dodecaene, C42H50O
9, adopts the 1,3-alternate conformation owing to the presence of a 1,3-pol
yether chain.